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Items: 1 to 20 of 109

1.

Stromal-derived factor-1 gene variations in pediatric patients with primary immune thrombocytopenia.

Ku FC, Tsai CR, Der Wang J, Wang CH, Chang TK, Hwang WL.

Eur J Haematol. 2013 Jan;90(1):25-30. doi: 10.1111/ejh.12025. Epub 2012 Dec 11.

PMID:
23078136
2.

Investigation of TNF-alpha, TGF-beta 1, IL-10, IL-6, IFN-gamma, MBL, GPIA, and IL1A gene polymorphisms in patients with idiopathic thrombocytopenic purpura.

Pehlivan M, Okan V, Sever T, Balci SO, Yilmaz M, Babacan T, Pehlıvan S.

Platelets. 2011;22(8):588-95. doi: 10.3109/09537104.2011.577255. Epub 2011 May 19.

PMID:
21591983
3.

Stromal cell-derived factor-1 rs2297630 polymorphism associated with platelet production and treatment response in Chinese patients with chronic immune thrombocytopenia.

Lyu M, Li Y, Hao Y, Sun T, Liu W, Lyu C, Fu R, Li H, Xue F, Liu X, Zhang L, Yang R.

Platelets. 2016 Jun;27(4):338-43. doi: 10.3109/09537104.2015.1103368. Epub 2015 Nov 20.

PMID:
26587874
4.

The role of PTPN22 gene polymorphism in childhood immune thrombocytopenic purpura.

Anis SK, Abdel Ghany EA, Mostafa NO, Ali AA.

Blood Coagul Fibrinolysis. 2011 Sep;22(6):521-5. doi: 10.1097/MBC.0b013e328347b064.

PMID:
21597364
5.

Cannabinoid CB2 receptor gene (CNR2) polymorphism is associated with chronic childhood immune thrombocytopenia in Egypt.

Mahmoud Gouda H, Mohamed Kamel NR.

Blood Coagul Fibrinolysis. 2013 Apr;24(3):247-51. doi: 10.1097/MBC.0b013e32835aba1d.

PMID:
23406660
6.

DNA methyltransferase 3B (DNMT3B -579G>T) promotor polymorphism and the susceptibility to pediatric immune thrombocytopenic purpura in Egypt.

Khorshied MM, El-Ghamrawy MK.

Gene. 2012 Dec 10;511(1):34-7. doi: 10.1016/j.gene.2012.09.024. Epub 2012 Sep 18.

PMID:
23000068
7.

DNMT3B promoter polymorphism and risk of immune thrombocytopenic purpura in pediatric Egyptians.

Shaheen IA, Abukhalil RE, Ali DK, Afifi RA.

Blood Coagul Fibrinolysis. 2012 Oct;23(7):636-9.

PMID:
22885766
8.

PTPN22 -1123G > C polymorphism is associated with susceptibility to primary immune thrombocytopenia in Chinese population.

Ge J, Li H, Gu D, Du W, Xue F, Sui T, Xu J, Yang R.

Platelets. 2013;24(6):448-53. doi: 10.3109/09537104.2012.730646. Epub 2012 Oct 25.

PMID:
23098231
9.

STAT1 single nucleotide polymorphisms and susceptibility to immune thrombocytopenia.

Chen Z, Guo Z, Ma J, Liu F, Gao C, Liu S, Wang A, Wu R.

Autoimmunity. 2015;48(5):305-12. doi: 10.3109/08916934.2015.1016218. Epub 2015 Feb 24.

PMID:
25707685
10.

Polymorphisms of the IL-23R gene are associated with primary immune thrombocytopenia but not with the clinical outcome of pulsed high-dose dexamethasone therapy.

Zhan Y, Hua F, Ji L, Wang W, Zou S, Wang X, Li F, Cheng Y.

Ann Hematol. 2013 Aug;92(8):1057-62. doi: 10.1007/s00277-013-1731-3. Epub 2013 Apr 7.

PMID:
23564312
11.

Stromal cell-derived factor-1 (SDF-1/CXCL12) gene polymorphisms in pulmonary tuberculosis patients of south India.

Selvaraj P, Alagarasu K, Singh B.

Int J Immunogenet. 2012 Feb;39(1):26-31. doi: 10.1111/j.1744-313X.2011.01059.x. Epub 2011 Nov 12.

PMID:
22077991
12.

Association of cytotoxic T-lymphocyte antigen 4 gene polymorphisms with idiopathic thrombocytopenic purpura in a Chinese population.

Li H, Ge J, Zhao H, Du W, Xu J, Sui T, Ma L, Zhou Z, Qi A, Yang R.

Platelets. 2011;22(1):39-44. doi: 10.3109/09537104.2010.521601. Epub 2010 Oct 29.

PMID:
21034161
13.

Interferon-gamma +874A/T and interleukin-4 intron3 VNTR gene polymorphisms in Chinese patients with idiopathic thrombocytopenic purpura.

Chen X, Xu J, Chen Z, Zhou Z, Feng X, Zhou Y, Ren Q, Yang R, Han ZC.

Eur J Haematol. 2007 Sep;79(3):191-7. Epub 2007 Jul 26.

PMID:
17655693
14.

Interleukin-27 rs153109 polymorphism and the risk for immune thrombocytopenia.

Zhao H, Zhang Y, Xue F, Xu J, Fang Z.

Autoimmunity. 2013 Dec;46(8):509-12. doi: 10.3109/08916934.2013.822072. Epub 2013 Aug 12.

PMID:
23937109
15.

FcγRIIa and FcγRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome.

Papagianni A, Economou M, Tragiannidis A, Karatza E, Samarah F, Gombakis N, Athanassiadou-Piperopoulou F, Vavatsi-Christaki N, Athanassiou-Metaxa M.

Blood Coagul Fibrinolysis. 2013 Jan;24(1):35-9. doi: 10.1097/MBC.0b013e328359bc3b.

PMID:
23249566
16.

FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt.

Eyada TK, Farawela HM, Khorshied MM, Shaheen IA, Selim NM, Khalifa IA.

Blood Coagul Fibrinolysis. 2012 Jan;23(1):64-8. doi: 10.1097/MBC.0b013e32834ddf2f.

PMID:
22123287
17.

[Relationship between polymorphisms of FCGR2B and susceptibility of children idiopathic thrombocytopenic purpura].

He LY, Huang YJ, Lai DB, Zhao MB, Zhang WY, Xu T, Wang JY, Shi J, Zhao YH, Xu XX.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2009 Jun;17(3):729-33. Chinese.

PMID:
19549396
18.

Single nucleotide polymorphism in the methyl-CpG binding domain 4 gene and the risk for immune thrombocytopenic purpura in Chinese population.

Zhao H, Du W, Wang D, Gu D, Xue F, Ge J, Sui T, Yang R.

Platelets. 2010;21(2):132-6. doi: 10.3109/09537100903474365.

PMID:
20100009
19.

Has-mir-146a rs2910164 polymorphism and risk of immune thrombocytopenia.

Zhao H, Zhang Y, Xue F, Xu J, Fang Z.

Autoimmunity. 2014 May;47(3):173-6. doi: 10.3109/08916934.2014.883503. Epub 2014 Feb 6.

PMID:
24502829
20.

Interleukin-18 gene promoter--607 A/C polymorphism and the risk of immune thrombocytopenia.

Zhao H, Zhang Y, Xiao G, Wu N, Xu J, Fang Z.

Autoimmunity. 2014 Nov;47(7):478-81. doi: 10.3109/08916934.2014.921812. Epub 2014 Jun 4.

PMID:
24897237

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